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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587424Generated: November 1, 2026

Anthranilic Acid → HCID 19757766, compound

https://huagongshe.com/reaction/1587424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 18547076HCID 18547076—
SolventSodium HydroxideHCID 14798—
ProductHCID 19757766HCID 19757766957.3%

Reaction Steps

3-Methylbenzenethiol and butyl bromoacetate were reacted by a conventional method and then hydrolyzed to obtain 3-methyl-α-phenylthioacetatic acid. 3-Methyl-α-phenylthioacetatic acid was reacted with thionyl chloride by a conventional method to obtain 3-methyl-α-phenylthioacetyl chloride. Anthranilic acid 5.6 g (4.1 mmol) was dissolved in 10% aqueous sodium hydroxide solution 32 ml and to this solution, 3-methyl-α-phenylthioacetyl chloride (99° C./3.3 mmHg) 8.9 g was added dropwise at 0° C. The resulting solution was stirred at room temperature for 20 minutes and neutralized with 10% hydrochloric acid solution. To this solution, ether was added, and deposited crystals were collected by filtration and washed with hot water to obtain N-(3-methylphenylthioacetyl)anthranilic acid (melting point: 148° to 150° C.) 11.2 g (yield: 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217961
Source datasetuspto-grants-1993_06
ORD IDord-8811d0e39015425499e95752035af04e
Source noteuspto-grants-1993_06